| Year |
Citation |
Score |
| 2011 |
Stopa JD, Chandani S, Tolan DR. Stabilization of the predominant disease-causing aldolase variant (A149P) with zwitterionic osmolytes. Biochemistry. 50: 663-71. PMID 21166391 DOI: 10.1021/Bi101523X |
0.711 |
|
| 2010 |
Coffee EM, Tolan DR. Mutations in the promoter region of the aldolase B gene that cause hereditary fructose intolerance. Journal of Inherited Metabolic Disease. 33: 715-25. PMID 20882353 DOI: 10.1007/S10545-010-9192-5 |
0.701 |
|
| 2010 |
Funari VA, Voevodski K, Leyfer D, Yerkes L, Cramer D, Tolan DR. Quantitative gene expression profiles in real time from expressed sequence tag databases. Gene Expression. 14: 321-36. PMID 20635574 DOI: 10.3727/105221610X12717040569820 |
0.578 |
|
| 2010 |
Coffee EM, Yerkes L, Ewen EP, Zee T, Tolan DR. Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population. Journal of Inherited Metabolic Disease. 33: 33-42. PMID 20033295 DOI: 10.1007/S10545-009-9008-7 |
0.693 |
|
| 2008 |
Sherawat M, Tolan DR, Allen KN. Structure of a rabbit muscle fructose-1,6-bisphosphate aldolase A dimer variant Acta Crystallographica Section D: Biological Crystallography. 64: 543-550. PMID 18453690 DOI: 10.1107/S0907444908004976 |
0.329 |
|
| 2007 |
Pezza JA, Stopa JD, Brunyak EM, Allen KN, Tolan DR. Thermodynamic analysis shows conformational coupling and dynamics confer substrate specificity in fructose-1,6-bisphosphate aldolase Biochemistry. 46: 13010-13018. PMID 17935305 DOI: 10.1021/Bi700713S |
0.645 |
|
| 2007 |
Funari VA, Crandall JE, Tolan DR. Fructose metabolism in the cerebellum. Cerebellum (London, England). 6: 130-40. PMID 17510913 DOI: 10.1080/14734220601064759 |
0.591 |
|
| 2005 |
Funari VA, Herrera VL, Freeman D, Tolan DR. Genes required for fructose metabolism are expressed in Purkinje cells in the cerebellum. Brain Research. Molecular Brain Research. 142: 115-22. PMID 16266770 DOI: 10.1016/J.Molbrainres.2005.09.019 |
0.602 |
|
| 2005 |
Malay AD, Allen KN, Tolan DR. Structure of the thermolabile mutant aldolase B, A149P: Molecular basis of hereditary fructose intolerance Journal of Molecular Biology. 347: 135-144. PMID 15733923 DOI: 10.1016/J.Jmb.2005.01.008 |
0.342 |
|
| 2004 |
Arakaki TL, Pezza JA, Cronin MA, Hopkins CE, Zimmer DB, Tolan DR, Allen KN. Structure of human brain fructose 1,6-(bis)phosphate aldolase: linking isozyme structure with function. Protein Science : a Publication of the Protein Society. 13: 3077-84. PMID 15537755 DOI: 10.1110/Ps.04915904 |
0.717 |
|
| 2004 |
Pezza JA, Allen KN, Tolan DR. Intein-mediated purification of a recombinantly expressed peptide Chemical Communications. 10: 2412-2413. PMID 15514791 DOI: 10.1039/B407924H |
0.664 |
|
| 2003 |
Pezza JA, Choi KH, Berardini TZ, Beernink PT, Allen KN, Tolan DR. Spatial clustering of isozyme-specific residues reveals unlikely determinants of isozyme specificity in fructose-1,6-bisphosphate aldolase Journal of Biological Chemistry. 278: 17307-17313. PMID 12611890 DOI: 10.1074/Jbc.M209185200 |
0.72 |
|
| 2002 |
Malay AD, Procious SL, Tolan DR. The temperature dependence of activity and structure for the most prevalent mutant aldolase B associated with hereditary fructose intolerance. Archives of Biochemistry and Biophysics. 408: 295-304. PMID 12464284 DOI: 10.1016/S0003-9861(02)00546-5 |
0.315 |
|
| 2001 |
Choi KH, Shi J, Hopkins CE, Tolan DR, Allen KN. Snapshots of catalysis: The structure of fructose-1,6-(bis)phosphate aldolase covalently bound to the substrate dihydroxyacetone phosphate Biochemistry. 40: 13868-13875. PMID 11705376 DOI: 10.1021/Bi0114877 |
0.32 |
|
| 2001 |
Dalby AR, Tolan DR, Littlechild JA. The structure of human liver fructose-1,6-bisphosphate aldolase. Acta Crystallographica. Section D, Biological Crystallography. 57: 1526-33. PMID 11679716 DOI: 10.1107/S0907444901012719 |
0.317 |
|
| 1999 |
Choi KH, Mazurkie AS, Morris AJ, Utheza D, Tolan DR, Allen KN. Structure of a fructose-1,6-bis(phosphate) aldolase liganded to its natural substrate in a cleavage-defective mutant at 2.3 Å Biochemistry. 38: 12655-12664. PMID 10504235 DOI: 10.1021/Bi9828371 |
0.336 |
|
| 1995 |
Doyle SA, Tolan DR. Characterization of recombinant human aldolase B and purification by metal chelate chromatography Biochemical and Biophysical Research Communications. 206: 902-908. PMID 7832803 DOI: 10.1006/bbrc.1995.1128 |
0.314 |
|
| 1994 |
Brooks CC, Tolan DR. A partially active mutant aldolase B from a patient with hereditary fructose intolerance Faseb Journal. 8: 107-113. PMID 8299883 |
0.334 |
|
| 1993 |
Morris AJ, Tolan DR. Site-directed mutagenesis identifies aspartate 33 as a previously unidentified critical residue in the catalytic mechanism of rabbit aldolase A Journal of Biological Chemistry. 268: 1095-1100. PMID 8419316 |
0.323 |
|
| 1991 |
Brooks CC, Buist N, Tuerck J, Tolan DR. Identification of a splice-site mutation in the aldolase B gene from an individual with hereditary fructose intolerance American Journal of Human Genetics. 49: 1075-1081. PMID 1928090 |
0.304 |
|
| 1988 |
Cross NCP, Tolan DR, Cox TM. Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation Cell. 53: 881-885. PMID 3383242 DOI: 10.1016/S0092-8674(88)90349-2 |
0.32 |
|
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